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More about Kyle

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Kyle is a 17 yr. old boy dealing with the # 1 most fatal disease in white American children: Cystic Fibrosis ( CF ).  CF is a hereditary disease that attacks primarily the lungs and digestive system. 

THERE IS NO CURE YOU CAN ONLY TREAT THE SYMPTOMS.

Kyle has endured 13 surgeries related to CF.  His most recent surgery was on June 15th.  Kyle required a feeding tube so his body can get all the nutrients it requires.  He spends weeks at a time in Riley Hospital for Children in Indpls. In.  This alone is a 4 hour trip one way......( Kyle must return to Riley every 2-3 weeks for check up visits )

On a daily basis Kyle does 6 aerosol and vest therapy treatments:

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10 hours connected to a intral feeding machine:

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Kyle must also take 39+pills daily...He wants nothing more than to be a normal 17 year old boy.  But recently Kyle was dealt yet another medical blow.  He may require a pancreas transplant within the next 2 years.  He also may need a lung transplant in 5-7 years.  Insurance does not cover all the medical expenses concerning a transplant. In addintion, there are mounting costs with medicines, trasnportation costs to and from Riley and the cost of Kyle's medical supplies.  We need your help....
Please join us on August 4th in South Bend, In at
 
 
Not only will you have a great time with live entertainment, dinner, tip boards, raffles and prizes but you will be helping a most deserving young man and the family who cares so deeply for him....

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